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FKRP anticorps (AA 237-265)

Cet anticorps anti-FKRP est un anticorps Lapin Polyclonal détectant FKRP dans WB. Adapté pour Humain.
N° du produit ABIN5536570

Aperçu rapide pour FKRP anticorps (AA 237-265) (ABIN5536570)

Antigène

Voir toutes FKRP Anticorps
FKRP (Fukutin Related Protein (FKRP))

Reactivité

  • 38
  • 14
  • 13
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 30
  • 8
Lapin

Clonalité

  • 30
  • 8
Polyclonal

Conjugué

  • 16
  • 5
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp FKRP est non-conjugé

Application

  • 25
  • 24
  • 4
  • 3
  • 2
Western Blotting (WB)
  • Épitope

    • 10
    • 6
    • 5
    • 5
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    AA 237-265

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    This FKRP antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 237-265 amino acids from the Central region of human FKRP.

    Isotype

    Ig Fraction
  • Indications d'application

    For WB starting dilution is: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Buffer

    Supplied in PBS with 0.09 % (W/V) sodium azide.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Antigène

    FKRP (Fukutin Related Protein (FKRP))

    Autre désignation

    FKRP

    Sujet

    This gene encodes a protein which is targeted to the medial Golgi apparatus and is necessary for posttranslational modification of dystroglycan. Mutations in this gene have been associated with congenital muscular dystrophy, mental retardation, and cerebellar cysts. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq].

    Poids moléculaire

    55 kDa

    ID gène

    79147

    UniProt

    Q9H9S5

    Pathways

    Regulation of Carbohydrate Metabolic Process
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